» Articles » PMID: 32032073

Risk of Tuberculosis in Patients With Inflammatory Bowel Disease on Infliximab or Adalimumab Is Dependent on the Local Disease Burden of Tuberculosis: A Systematic Review and Meta-Analysis

Overview
Specialty Gastroenterology
Date 2020 Feb 8
PMID 32032073
Citations 21
Authors
Affiliations
Soon will be listed here.
Abstract

Objectives: Infliximab (IFX) or adalimumab (ADA) use in patients with inflammatory bowel disease (IBD) leads to increased risk of tuberculosis (TB). This meta-analysis evaluated the factors which determine this risk, with special focus on local TB incidence.

Methods: All studies until January 31, 2019, which reported the development of TB in patients with IBD on IFX/ADA, were included after searching PubMed and Embase. Data regarding disease type, number of patients on IFX/ADA, number of patients who developed TB, mean age at IFX/ADA initiation, median duration of development of TB, and latent TB (LTB) were extracted. The details on local TB incidence were obtained from the World Health Organization database, and the studies were stratified into low (<10/100,000), intermediate (10-40/100,000), and high TB burden countries (>40/100,000). Random effect meta-analysis was performed to calculate the overall pooled prevalence and prevalence based on local TB burden.

Results: Of 130,114 patients (128 studies), 373 developed TB (pooled prevalence: 0.08% [95% confidence interval {CI}: 0.05%-0.10%]). The risk increased with increasing TB burden, pooled prevalence being 0.02% (95% CI: 0.02%-0.03%), 0.21% (95% CI: -0.02% to 0.43%), and 1.59% (95% CI: 1.19%-2.00%) for low, intermediate, and high TB burden countries, respectively. Seventy-three percent of patients who developed TB had no evidence of LTB on screening, the proportion being independent of TB burden. There was no effect of disease or treatment type, study type, gender, age at IFX/ADA initiation, and follow-up duration on TB prevalence.

Discussion: TB risk in patients with IBD on IFX/ADA depends on the local TB burden and is independent of disease/treatment type.

Citing Articles

Anti-Tumor Necrosis Factor-α Use in Pediatric Inflammatory Bowel Disease-Reports from a Romanian Center.

Matran R, Diaconu A, Iordache A, Dijmarescu I, Coroleuca A, Pacurar D Pharmaceuticals (Basel). 2025; 18(1).

PMID: 39861147 PMC: 11768541. DOI: 10.3390/ph18010084.


Peritoneal Tuberculosis Mimicking Ovarian Malignancy: A Case Report.

Al-Zughali E, Al-Shami N, Hamedat A, Al-Bustanji S, Almaletti M, Al-Shaibani E Cureus. 2025; 16(12):e76231.

PMID: 39845238 PMC: 11751587. DOI: 10.7759/cureus.76231.


The resolvin D2 and omega-3 polyunsaturated fatty acid as a new possible therapeutic approach for inflammatory bowel diseases.

Chaim F, Pascoal L, de Castro M, Palma B, Rodrigues B, Fagundes J Sci Rep. 2024; 14(1):28698.

PMID: 39562789 PMC: 11576872. DOI: 10.1038/s41598-024-80051-8.


Emerging Patterns of Inflammatory Bowel Disease in Sub-Saharan Africa: 175 Cases From an Inflammatory Bowel Disease Network.

Hodges P, Adeniyi O, Devani S, Nwoko C, Owoseni O, Boateng K J Crohns Colitis. 2024; 19(1).

PMID: 39140612 PMC: 11725509. DOI: 10.1093/ecco-jcc/jjae126.


Comparative risk of serious infections and tuberculosis in Korean patients with inflammatory bowel disease treated with non-anti-TNF biologics or anti-TNF-α agents: a nationwide population-based cohort study.

Kim M, Kim Y, Jeong D, Kim S, Hong S, Park S Therap Adv Gastroenterol. 2024; 17:17562848241265013.

PMID: 39092170 PMC: 11292712. DOI: 10.1177/17562848241265013.